Genome-Wide Association Study

Genetic Ancestry Markers and Difference in A1c Between African American and White in the Diabetes Prevention Program.

Hivert MF, Christophi CA, Jablonski KA, et al. Genetic Ancestry Markers and Difference in A1c Between African American and White in the Diabetes Prevention Program. J Clin Endocrinol Metab. 2019;104(2):328-336. doi:10.1210/jc.2018-01416

Candidate-based screening via gene modulation in human neurons and astrocytes implicates FERMT2 in Aβ and TAU proteostasis.

Sullivan SE, Liao M, Smith RV, et al. Candidate-based screening via gene modulation in human neurons and astrocytes implicates FERMT2 in Aβ and TAU proteostasis. Hum Mol Genet. 2019;28(5):718-735. doi:10.1093/hmg/ddy376

Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.

Ligthart S, Vaez A, Võsa U, et al. Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders. Am J Hum Genet. 2018;103(5):691-706. doi:10.1016/j.ajhg.2018.09.009

Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort.

Galván-Femenía I, Obón-Santacana M, Piñeyro D, et al. Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort. J Med Genet. 2018;55(11):765-778. doi:10.1136/jmedgenet-2018-105437

Genetic analysis of right heart structure and function in 40,000 people.

Pirruccello JP, Di Achille P, Nauffal V, et al. Genetic analysis of right heart structure and function in 40,000 people. Nat Genet. 2022;54(6):792-803. doi:10.1038/s41588-022-01090-3

Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume.

Vojinovic D, Adams HH, Jian X, et al. Genome-wide association study of 23,500 individuals identifies 7 loci associated with brain ventricular volume. Nat Commun. 2018;9(1):3945. doi:10.1038/s41467-018-06234-w

Genome-wide pleiotropy analysis of coronary artery disease and pneumonia identifies shared immune pathways.

Yu Z, Zekavat SM, Haidermota S, et al. Genome-wide pleiotropy analysis of coronary artery disease and pneumonia identifies shared immune pathways. Sci Adv. 2022;8(16):eabl4602. doi:10.1126/sciadv.abl4602

Improving Imputation Accuracy by Inferring Causal Variants in Genetic Studies.

Wu Y, Hormozdiari F, Joo JWJ, Eskin E. Improving Imputation Accuracy by Inferring Causal Variants in Genetic Studies. J Comput Biol. 2019;26(11):1203-1213. doi:10.1089/cmb.2018.0139

The Shared Genetic Basis of Educational Attainment and Cerebral Cortical Morphology.

Ge T, Chen CY, Doyle AE, et al. The Shared Genetic Basis of Educational Attainment and Cerebral Cortical Morphology. Cereb Cortex. 2019;29(8):3471-3481. doi:10.1093/cercor/bhy216

Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data.

Guo MH, Plummer L, Chan YM, Hirschhorn JN, Lippincott MF. Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data. Am J Hum Genet. 2018;103(4):522-534. doi:10.1016/j.ajhg.2018.08.016

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